Haemophilia

Haemophilia is a rare genetic disorder, affecting roughly 1 in every 5,000 male births. It is caused by an inherited deficiency in one of the clotting factors in the blood. People with haemophilia lack certain proteins which help to slow or stop the flow of blood. This can result in excessive bleeding, even from a minor wound. If left untreated, serious internal bleeding can occur, which can be life-threatening. Treatment options are available to help manage haemophilia and reduce the risks of excessive bleeding. In some cases, treatment may even allow people with the condition to live their lives without major disruption.

← International Journal of Blood Transfusion

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Acquired Haemophilia: A Case Report and Literature Review

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